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			Welcome!!! <br> <br> Massively parallel DNA sequencing is
			getting attention and is considering as a useful tool to identify
			causal genes of disease because of succession in identifying causal
			genes of some diseases. <br /> (Ng,S.B. et al. (2009), Nature, 461,
			272-276.) However, analysis and interpretation of sequence variation
			is a bottle-neck of NGS data even there are many commercial or public
			software. To solve the problem, <br /> pSEVA not only makes NGS data
			analysis easy including QC and filtering but also provides a detail of
			sequence variation by the integration of annotation databases and
			tools. <br /> Moreover, pSEVA offers a GUI interface with Web
			browser, and supports HPC(High Performance Computer) system with
			Oracle Grid Engine to speed up the analysis if it is available.
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